Phosphatidylserine targeted single-walled carbon nanotubes for photothermal ablation of bladder cancer

Bladder cancer has a 60%–70% recurrence rate most likely due to any residual tumour left behind after a transurethral resection (TUR). Failure to completely resect the cancer can lead to recurrence and progression into higher grade tumours with metastatic potential. We present here a novel therapy to treat superficial tumours with the potential to decrease recurrence. The therapy is a heat-based approach in which bladder tumour specific single-walled carbon nanotubes (SWCNTs) are delivered intravesically at a very low dose (0.1 mg SWCNT per kg body weight) followed 24 h later by a short 30 s treatment with a 360° near-infrared light that heats only the bound nanotubes. The energy density of the treatment was 50 J cm−2, and the power density that this treatment corresponds to is 1.7 W cm−2, which is relatively low. Nanotubes are specifically targeted to the tumour via the interaction of annexin V (AV) and phosphatidylserine, which is normally internalised on healthy tissue but externalised on tumours and the tumour vasculature. SWCNTs are conjugated to AV, which binds specifically to bladder cancer cells as confirmed in vitro and in vivo. Due to this specific localisation, NIR light can be used to heat the tumour while conserving the healthy bladder wall. In a short-term efficacy study in mice with orthotopic MB49 murine bladder tumours treated with the SWCNT-AV conjugate and NIR light, no tumours were visible on the bladder wall 24 h after NIR light treatment, and there was no damage to the bladder. In a separate survival study in mice with the same type of orthotopic tumours, there was a 50% cure rate at 116 days when the study was ended. At 116 days, no treatment toxicity was observed, and no nanotubes were detected in the clearance organs or bladder.

[1]  D. Lamm,et al.  BCG-unresponsive non-muscle-invasive bladder cancer: recommendations from the IBCG , 2017, Nature Reviews Urology.

[2]  Z. Hua,et al.  Anti-cancer activity of Annexin V in murine melanoma model by suppressing tumor angiogenesis , 2017, Oncotarget.

[3]  Jia-Jin Chen,et al.  Photo-thermal therapy of bladder cancer with Anti-EGFR antibody conjugated gold nanoparticles. , 2016, Frontiers in bioscience.

[4]  R. Birge,et al.  Phosphatidylserine is a global immunosuppressive signal in efferocytosis, infectious disease, and cancer , 2016, Cell Death and Differentiation.

[5]  J. McKiernan,et al.  Modelling bladder cancer in mice: opportunities and challenges , 2014, Nature Reviews Cancer.

[6]  Anton V. Liopo,et al.  Enabling in vivo measurements of nanoparticle concentrations with three‐dimensional optoacoustic tomography , 2014, Journal of biophotonics.

[7]  S. Torti,et al.  Carbon nanotubes in hyperthermia therapy. , 2013, Advanced drug delivery reviews.

[8]  R. Harrison,et al.  Purine Nucleoside Phosphorylase Targeted by Annexin V to Breast Cancer Vasculature for Enzyme Prodrug Therapy , 2013, PloS one.

[9]  R. Ramesh,et al.  Targeting single-walled carbon nanotubes for the treatment of breast cancer using photothermal therapy , 2013, Nanotechnology.

[10]  P. Hauser,et al.  Tryptase Activation of Immortalized Human Urothelial Cell Mitogen-Activated Protein Kinase , 2013, PloS one.

[11]  Prokar Dasgupta,et al.  Recent advances in the diagnosis and treatment of bladder cancer , 2013, BMC Medicine.

[12]  A. Seifalian,et al.  Synergistic photothermal ablative effects of functionalizing carbon nanotubes with a POSS-PCU nanocomposite polymer , 2012, Journal of Nanobiotechnology.

[13]  P. Ajayan,et al.  The resistance of breast cancer stem cells to conventional hyperthermia and their sensitivity to nanoparticle-mediated photothermal therapy. , 2012, Biomaterials.

[14]  D. Resasco,et al.  Vascular targeted single-walled carbon nanotubes for near-infrared light therapy of cancer , 2011, Nanotechnology.

[15]  Lucian Mocan,et al.  Advances in cancer therapy through the use of carbon nanotube-mediated targeted hyperthermia , 2011, International journal of nanomedicine.

[16]  Xiaoming He,et al.  Thermostability of Biological Systems: Fundamentals, Challenges, and Quantification , 2011, The open biomedical engineering journal.

[17]  H. Dai,et al.  High performance in vivo near-IR (>1 μm) imaging and photothermal cancer therapy with carbon nanotubes , 2010, Nano research.

[18]  M. Zeegers,et al.  Mechanisms of recurrence of Ta/T1 bladder cancer. , 2010, Annals of the Royal College of Surgeons of England.

[19]  C. Reutelingsperger,et al.  Phosphatidylserine targeting for diagnosis and treatment of human diseases , 2010, Apoptosis.

[20]  W. Larchian,et al.  Optimizing orthotopic bladder tumor implantation in a syngeneic mouse model. , 2009, The Journal of urology.

[21]  H. Choi,et al.  In vivo near-infrared mediated tumor destruction by photothermal effect of carbon nanotubes. , 2009, ACS nano.

[22]  R. Leapman,et al.  Imaging the distribution of individual platinum-based anticancer drug molecules attached to single-wall carbon nanotubes. , 2009, Nanomedicine.

[23]  J. Au,et al.  Intravesical Treatments of Bladder Cancer: Review , 2008, Pharmaceutical Research.

[24]  Weibo Cai,et al.  Circulation and long-term fate of functionalized, biocompatible single-walled carbon nanotubes in mice probed by Raman spectroscopy , 2008, Proceedings of the National Academy of Sciences.

[25]  H. Dai,et al.  Carbon nanotubes as multifunctional biological transporters and near-infrared agents for selective cancer cell destruction. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[26]  C. Christophi,et al.  Mechanisms of focal heat destruction of liver tumors. , 2005, The Journal of surgical research.

[27]  P. Thorpe,et al.  A monoclonal antibody that binds anionic phospholipids on tumor blood vessels enhances the antitumor effect of docetaxel on human breast tumors in mice. , 2005, Cancer research.

[28]  S. Ran,et al.  Antitumor Effects of a Monoclonal Antibody that Binds Anionic Phospholipids on the Surface of Tumor Blood Vessels in Mice , 2005, Clinical Cancer Research.

[29]  C. Reutelingsperger,et al.  Cell Surface-expressed Phosphatidylserine and Annexin A5 Open a Novel Portal of Cell Entry* , 2004, Journal of Biological Chemistry.

[30]  S. Ran,et al.  Phosphatidylserine is a marker of tumor vasculature and a potential target for cancer imaging and therapy. , 2002, International journal of radiation oncology, biology, physics.